Category: Featured

Micro Labs Ltd is inviting applications from experienced professionals for Quality Control (QC) and QC Microbiology positions.
The company is hiring for the designations of Senior Officer and Senior Executive, with opportunities in pharmaceutical quality control and microbiology.
Candidates with M.Pharm, B.Pharm, M.Sc, or M.Sc in Microbiology can apply for the relevant positions based on their qualifications and experience.
The job location is Micro Labs Ltd, Pharmaceutical Formulation Unit, Upper Mamring, South Sikkim, where selected candidates will work in quality control operations.

Micro Labs Ltd Recruitment: Company Overview

Micro Labs Ltd is a pharmaceutical company involved in healthcare and pharmaceutical manufacturing. The current recruitment announcement lists openings in Quality Control and QC Microbiology for candidates with relevant pharmaceutical or microbiology qualifications.

Micro Labs Ltd QC Vacancies and Job Details

1. Senior Officer / Senior Executive – Quality Control (QC)

Department: Quality Control (QC)

Designation: Senior Officer / Senior Executive

Qualification: M.Pharm / B.Pharm / M.Sc

Experience: 3–7 years

This position is intended for professionals with relevant qualifications and experience in pharmaceutical quality control.

2. Senior Officer / Executive – QC Microbiology

Department: Quality Control (Microbiology)

Designation: Senior Officer / Executive

Qualification: M.Sc in Microbiology

Experience: 1–5 years

This opportunity is suitable for microbiology professionals seeking roles in pharmaceutical quality control and microbiological operations.

Eligibility & Qualifications

Candidates must meet the qualification and experience requirements specified for the relevant position.

Educational Qualifications

• M.Pharm
• B.Pharm
• M.Sc
• M.Sc in Microbiology

Experience Requirements

• QC: 3–7 years
• QC Microbiology: 1–5 years

Candidates should select the position that matches their educational background and relevant industry experience.

Job Location and Salary

Work Location: Micro Labs Ltd, Pharmaceutical Formulation Unit, Upper Mamring, South Sikkim – 737132.

The recruitment announcement does not specify salary details. Compensation may depend on the selected position, relevant experience, and company policy.

How to Apply for Micro Labs Ltd Recruitment

Interested candidates can send their updated resumes to the recruitment contact provided in the announcement.

Email: santu.pal@microlabs.in

Contact Number: 6294339843

Applicants should mention the position they are applying for and include their qualifications, experience, and updated contact details in their resumes.

Documents to Keep Ready

Candidates should prepare the following documents for the recruitment process:

• Updated resume or CV
• Educational qualification certificates
• Relevant experience certificates
• Previous employment details, if applicable
• Valid contact details

Frequently Asked Questions

1. Which positions are available at Micro Labs Ltd?

The openings are for Senior Officer / Senior Executive in QC and Senior Officer / Executive in QC Microbiology.

2. What qualifications are required for QC jobs?

Candidates with M.Pharm, B.Pharm, or M.Sc qualifications are eligible for the QC position, subject to the relevant experience requirements.

3. Is M.Sc Microbiology required for QC Microbiology?

Yes. The announcement specifies M.Sc in Microbiology for the QC Microbiology position.

4. How much experience is required?

The QC position requires 3–7 years of experience, while QC Microbiology requires 1–5 years.

5. Where is the job location?

The work location is Micro Labs Ltd, Pharmaceutical Formulation Unit, Upper Mamring, South Sikkim – 737132.

6. How can candidates apply?

Candidates can email their updated resumes to santu.pal@microlabs.in or contact 6294339843.

Job Summary

Category	Details
Company	Micro Labs Ltd
Vacancies	Senior Officer / Senior Executive – QC; Senior Officer / Executive – QC Microbiology
Required Education	M.Pharm, B.Pharm, M.Sc, M.Sc Microbiology
Experience	QC: 3–7 years; QC Microbiology: 1–5 years

 

Lupin Walk-In Interview 2026 | Biotechnology, Biologics, Production, Engineering and GMP Compliance

Lupin is conducting a walk-in interview for experienced professionals in its Biotechnology Division and pharmaceutical manufacturing operations.
The recruitment drive covers Upstream and Downstream Production, Filling and Packaging, Visual Inspection, Engineering and Maintenance, and GMP Compliance.
Candidates with 2 to 10 years of relevant experience in biologics or biopharmaceuticals can apply for suitable opportunities.
The walk-in interview will be held on 25 October 2026 at Lemon Tree Hotel, Electronics City, Bengaluru, Karnataka.

Lupin Walk-In Interview: Company Overview

Lupin is inviting experienced candidates to explore opportunities across biotechnology, biopharmaceutical manufacturing, drug product manufacturing, engineering, and GMP compliance functions.

Lupin Recruitment 2026: Departments and Job Responsibilities

1. Biotechnology Division: Upstream and Downstream Production

The Upstream and Downstream Production function covers bioprocess manufacturing operations involving:

• Single-use bioreactors
• Fermenters
• Centrifuges
• Homogenizers
• Tangential Flow Filtration (TFF)
• Chromatography systems
• Aseptic filtration

2. Filling, Packaging and Visual Inspection

The Drug Product Manufacturing function includes filling, sterilization, packaging, and inspection operations.

Key areas include:

• Steam sterilization and filling machine operation
• Secondary packaging
• Pre-filled syringe (PFS) and vial labelling
• Blister packaging
• Check weighing
• Serialization

3. Engineering and Maintenance

The Engineering and Maintenance function covers pharmaceutical plant utilities, equipment maintenance, and technical support.

Key areas include:

• Water systems and pretreatment
• Purified Water (PW) and Water for Injection (WFI) systems
• Purified steam systems
• Calibration and alarm management
• Troubleshooting
• Instrumentation
• Heating, Ventilation and Air Conditioning (HVAC)
• Temperature mapping
• Spare parts management

4. GMP Compliance

The GMP Compliance function focuses on manufacturing compliance, quality systems, and validation activities.

Key areas include:

• Manufacturing GMP compliance
• Change control
• Deviation management
• Risk assessment
• Contamination Control Strategy (CCS)
• Cleaning validation
• Equipment qualification
• Computerized System Validation (CSV)

Eligibility and Qualifications for Lupin Recruitment

Experience Requirements

• Relevant experience: 2 to 10 years in biologics or biopharmaceuticals.

Preferred Educational Qualifications

• M.Sc. in Biotechnology or Microbiology
• M.Pharm
• B.Pharm
• B.Tech
• B.Sc. in Chemistry
• B.E. in Mechanical Engineering
• B.E. in Instrumentation Engineering
• B.E. in Electrical Engineering
• B.E. in Electronics and Telecommunication (E&TC)
• Diploma in Pharmacy
• Diploma in Mechanical Engineering
• Diploma in Electrical Engineering
• Diploma in Instrumentation Engineering
• Diploma in Electronics and Telecommunication (E&TC)
• Diploma in Chemical Engineering

Candidates should have relevant technical experience suited to the department and responsibilities they wish to pursue.

Lupin Walk-In Interview Details

Date and Time

• Date: Sunday, 25 October 2026
• Time: 9:00 AM to 5:30 PM
• Interview availability: Candidates can attend at any time during the stated interview hours.

Interview Venue

Lemon Tree Hotel, Electronics City

54B/55A, Hosur Main Road, Phase 1, Electronics City, Bengaluru – 560100, Karnataka, India.

How to Apply

Eligible candidates with 2 to 10 years of relevant experience in biologics or biopharmaceuticals can attend the walk-in interview directly at the specified venue.

Candidates should carry an updated resume and relevant educational and employment documents. The recruitment information provided does not specify an application email address or online registration link.

Documents to Carry

Candidates should prepare the following documents for the interview:

• Updated resume
• Educational certificates
• Relevant experience certificates
• Employment records and other supporting documents

Frequently Asked Questions

1. What is the experience requirement for Lupin recruitment?

Candidates should have 2 to 10 years of relevant experience in biologics or biopharmaceuticals.

2. Which qualifications are preferred?

Preferred qualifications include M.Sc. Biotechnology, M.Sc. Microbiology, M.Pharm, B.Pharm, B.Tech, B.Sc. Chemistry, relevant engineering degrees, and relevant diploma qualifications.

3. When is the Lupin walk-in interview?

The walk-in interview is scheduled for Sunday, 25 October 2026.

4. What are the interview timings?

Candidates can attend between 9:00 AM and 5:30 PM.

5. Where is the interview venue?

The interview will take place at Lemon Tree Hotel, Electronics City, Hosur Main Road, Bengaluru, Karnataka.

6. Can candidates attend at any time during the interview?

Yes. The announcement states that candidates can attend at any time throughout the scheduled interview day.

Job Summary

Category	Details
Company	Lupin
Vacancies	Biotechnology Production, Filling and Packaging, Visual Inspection, Engineering and Maintenance, GMP Compliance
Required Education	M.Sc. Biotechnology/Microbiology, M.Pharm, B.Pharm, B.Tech, B.Sc. Chemistry, relevant B.E. and Diploma qualifications
Experience	2–10 years in biologics or biopharmaceuticals

Navin Molecular Recruitment – Production Officer & Senior Officer Walk-In Interview 2026

Navin Molecular is conducting a walk-in interview on 24 October 2026 for Officer – Production and Senior Officer – Production positions at its manufacturing facility in Dewas, Madhya Pradesh. Candidates with qualifications in Chemical Engineering or Chemistry can apply, with experience requirements ranging from 0–4 years for Officer – Production and 5–6 years for Senior Officer – Production. Applicants should have hands-on experience in batch processing within chemical, pharmaceutical, API, intermediate, or specialty chemical manufacturing environments. Interested candidates should attend the interview with a hard copy of their CV or email their resumes if unable to attend in person.

Company Overview

Navin Molecular is a contract development and manufacturing organization (CDMO) providing services to pharmaceutical clients. It belongs to the Padmanabh Mafatlal Group and operates as part of Navin Fluorine International Limited’s manufacturing network. The Dewas facility supports CDMO services for pharmaceutical clients worldwide.

Job Details

Available Positions & Qualifications

1. Officer – Production

• Qualification: B.Tech, Diploma in Chemical Engineering, or M.Sc. Chemistry.

• Experience: 0–4 years.

• Suitable candidates: Applicants with relevant manufacturing or batch-processing experience in chemical, pharmaceutical, API, intermediate, or specialty chemical operations.

2. Senior Officer – Production

• Qualification: B.Tech, Diploma in Chemical Engineering, or M.Sc. Chemistry.

• Experience: 5–6 years.

• Suitable candidates: Experienced professionals with hands-on production and batch-processing expertise in chemical or pharmaceutical manufacturing.

Job Responsibilities & Technical Requirements

The recruitment announcement highlights the following responsibilities and technical expectations:

• Work in rotational shifts and participate actively in shop-floor manufacturing operations.

• Perform batch-processing activities in chemical, pharmaceutical, API, intermediate, or specialty chemical manufacturing environments.

• Work with unit operations such as distillation, crystallization, extraction, filtration, drying, and solvent recovery.

• Handle processes involving high-pressure or high-temperature reactions.

• Monitor process parameters during manufacturing operations.

• Ensure compliance with current Good Manufacturing Practices (cGMP) and safety requirements.

• Troubleshoot process deviations and support corrective actions.

• Contribute to efficient batch execution while maintaining product quality and productivity targets.

Eligibility & Qualifications

Candidates should possess one of the following qualifications:

B.Tech in Chemical Engineering, Diploma in Chemical Engineering, or M.Sc. Chemistry.

Experience requirements depend on the position:

• Officer – Production: 0–4 years.

• Senior Officer – Production: 5–6 years.

Hands-on manufacturing experience in relevant chemical or pharmaceutical operations is an important requirement.

Walk-In Interview Details

Required Documents

– Hard copy of your updated CV.

Candidates who cannot attend the interview in person may email their CVs to the recruitment address.

How to Apply

Interested candidates can attend the walk-in interview directly at the Dewas manufacturing facility on 24 October 2026, between 10:00 AM and 2:00 PM.

Candidates unable to attend in person can email their CV to:

Email: careers.dewas@navinmolecular.com

Applicants should mention the position they are applying for — Officer – Production or Senior Officer – Production — and highlight their relevant manufacturing experience.

Job Summary

Sun Pharma Recruitment – Officer QC / Production

Sun Pharma is hiring Officer – QC / Production professionals for its API pharmaceutical operations in Madurantakam and Chengalpattu, Tamil Nadu. Candidates with 2–5 years of relevant experience in Quality Control (QC) or Production in the API pharmaceutical industry are eligible to apply. The company is seeking candidates with qualifications in Chemistry, Pharmacy, or Chemical Engineering, with preference for immediate joiners. Interested candidates can share their updated resumes directly with the recruitment contact.

Company Overview

Sun Pharmaceutical Industries is a global pharmaceutical company focused on providing quality medicines and improving patient health. This recruitment opportunity is for professionals interested in QC or Production roles within the active pharmaceutical ingredient (API) industry.

Job Details

Eligibility & Qualifications

Candidates should possess one of the following qualifications:

• B.Sc. Chemistry

• M.Sc. Chemistry

• B.Pharm

• Diploma in Chemical Engineering

Experience Requirements

• 2–5 years of relevant experience in Quality Control or Production.

• Experience must be relevant to the API pharmaceutical industry.

• Immediate joiners are preferred.

Job Responsibilities

The recruitment announcement does not provide detailed responsibilities for the Officer – QC / Production position. Candidates should confirm the specific duties with the recruitment team.

Depending on the assigned role, relevant experience in pharmaceutical QC or API Production will be important.

Job Location

The openings are for the following locations in Tamil Nadu:

• Madurantakam

• Chengalpattu

How to Apply

Interested and eligible candidates can send their updated resumes to the recruitment email address.

• Email: seema.m1@sunpharma.com

• Suggested email subject: Application for Officer – QC / Production

Candidates should highlight their qualifications, API industry experience, QC or Production expertise, and availability to join in their applications.

Job Summary

Apitoria Pharma Recruitment – Quality Control (QC) Professionals

Apitoria Pharma Private Limited, a 100% subsidiary of Aurobindo Pharma Limited, is hiring experienced Quality Control (QC) professionals for its Active Pharmaceutical Ingredients (API) division in Visakhapatnam, Andhra Pradesh. Candidates with 3–6 years of experience and qualifications in M.Sc. Chemistry, M.Sc. Microbiology, or B.Pharmacy are invited to apply. The opportunity is suitable for professionals with knowledge of HPLC, GC, Quality Management Systems (QMS), microbiology, and pharmaceutical quality regulations. Interested candidates can submit their resumes directly to the recruitment team.

Company Overview

Apitoria Pharma Private Limited is a wholly owned subsidiary of Aurobindo Pharma Limited. The company is recruiting experienced QC professionals for its API division at its Visakhapatnam location.

Job Details

Job Role & Responsibilities

The selected candidates will support Quality Control activities in the API division.

Key responsibilities based on the recruitment announcement include:

• Perform analytical testing and related Quality Control activities.

• Work with analytical instruments and techniques, including HPLC and GC.

• Support Quality Management System (QMS) activities.

• Apply microbiological testing knowledge where relevant to assigned responsibilities.

• Maintain accurate quality documentation.

• Handle investigations related to QC activities.

• Follow current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), data integrity requirements, and applicable regulatory standards.

Eligibility & Qualifications

Candidates should possess one of the following qualifications:

M.Sc. Chemistry, M.Sc. Microbiology, or B.Pharmacy.

Experience Requirements

• 3–6 years of relevant experience in Quality Control.

• Experience in analytical testing, documentation, and investigation handling.

• Familiarity with pharmaceutical quality systems and regulatory requirements.

Required Skills

Applicants should have good knowledge of:

• High-Performance Liquid Chromatography (HPLC).

• Gas Chromatography (GC).

• Quality Management Systems (QMS).

• Microbiology.

• Current Good Manufacturing Practices (cGMP).

• Good Laboratory Practices (GLP).

• Data integrity and regulatory requirements.

• Analytical testing and quality documentation.

• Investigation handling.

Job Location

The positions are for the API division in Visakhapatnam, Andhra Pradesh, India.

How to Apply

Interested candidates with relevant Quality Control experience can send their updated resumes directly to the recruitment contact.

• Email: arunkumar.komshetpally@apitoria.com

• Suggested email subject: Application for QC Position – API Division, Visakhapatnam

Candidates should highlight their experience with HPLC, GC, QMS, analytical testing, documentation, and investigation handling in their resumes.

Job Summary

Fortrea Recruitment – Site Navigator I

Fortrea is hiring a Site Navigator I for its clinical research operations in India. This full-time opportunity is available to candidates based in Bangalore, Hyderabad, Pune, Mumbai, and other locations across India through a remote working arrangement. The role focuses on clinical trial site start-up, feasibility assessments, regulatory submissions, essential document management, and site activation. Candidates with a relevant degree or equivalent experience, knowledge of ICH-GCP guidelines, and experience in clinical research or related fields can apply.

Company Overview

Fortrea is a global clinical research services company supporting pharmaceutical and biotechnology organizations in clinical development. The Site Navigator I role helps coordinate investigative site activities, maintain regulatory compliance, and support the timely initiation and management of clinical studies.

Job Details

Job Role & Responsibilities

The Site Navigator I will coordinate clinical trial site activities from feasibility and initial outreach through site activation and, when required, study closeout. The role serves as a primary point of contact for investigative sites and supports collaboration between sponsors, CRO teams, and site staff.

Key responsibilities include:

• Coordinate site-level tasks for efficient site activation in compliance with ICH-GCP guidelines, local regulations, SOPs, and project requirements.

• Identify potential research sites and assess their capabilities, resources, and suitability for clinical studies.

• Conduct initial site outreach, obtain confidentiality agreements, and collect feasibility surveys.

• Perform remote pre-study visits, prepare visit documentation, and complete trip reports.

• Support customization and translation of informed consent forms (ICFs) and patient-facing materials.

• Collect, track, and quality-check essential documents required for site selection, regulatory submissions, and site activation.

• Monitor site regulatory compliance, including applicable ethics committee renewals, principal investigator changes, and document expirations.

• Participate in study team meetings and develop action plans for site-level risks, delays, and performance issues.

• Support Clinical Research Associate (CRA) teams in preparing for Site Initiation Visits (SIVs).

• Coordinate clinical study supplies, access requirements, and documentation with vendors and study teams.

• Prepare submissions to and liaise with Institutional Review Boards (IRBs), Independent Ethics Committees (IECs), third bodies where applicable, and regulatory authorities.

• Collaborate with Global Regulatory Submissions Leads on regulatory submissions.

• Conduct initial site contract and budget negotiations, including amendments where applicable.

• Maintain accurate essential documents and keep the Trial Master File (TMF) audit-ready.

• Track site start-up progress and ensure that milestones and deadlines are met.

• Serve as the primary contact for investigative sites and support timely delivery within the study scope and budget.

• Perform Case Report Form (CRF) reviews and validate clinical data against source documentation, as applicable.

• Support monitoring of protocol deviations, Serious Adverse Event (SAE) reporting, and other study activities as assigned.

Eligibility & Qualifications

Candidates should meet one of the qualification pathways specified by Fortrea:

• University or college degree, preferably in Life Sciences.

• Certification in a related allied health profession from an accredited institution, such as nursing, medical technology, or laboratory technology.

• Alternatively, 2–3 years of work experience in clinical research, including working knowledge of ICH-GCP guidelines and regulatory authority and IRB/IEC regulations.

• Fortrea may consider relevant equivalent experience instead of the stated educational requirements.

• Candidates with a high school diploma or equivalent and at least 5 years of clinical research experience, including strong knowledge of ICH-GCP and regulatory and IRB/IEC requirements, may also be considered under the alternative pathway.

Candidates must be fluent in the relevant local official language and English, both written and spoken.

Experience Requirements

Fortrea identifies the following experience and knowledge as important for this role:

• At least one year of experience in a related field, such as medical, clinical, pharmaceutical, or laboratory research, data analysis, data management, or technical writing.

• One year of clinical research experience is preferred.

• Basic knowledge of ICH-GCP, regulatory authority requirements, IRB/IEC regulations, and applicable clinical research guidelines.

• Familiarity with investigator site start-up documents and contract and budget negotiations.

• Understanding of clinical research protocols and study requirements.

• Experience interacting with operational project teams and investigative sites is preferred.

Required Skills & Competencies

Applicants should demonstrate:

• Strong written and verbal communication skills.

• Ability to coordinate with site staff, CRO personnel, sponsors, and regulatory authorities.

• Effective organization and time management.

• Ability to manage multiple tasks, competing priorities, and deadlines.

• Understanding of clinical trial regulations and compliance requirements.

• Problem-solving skills to identify and resolve site start-up issues.

• Ability to support site contract and budget negotiations.

• Attention to detail in regulatory documentation and Trial Master File maintenance.

Work Location & Environment

The position is remote-based in India, with possible office presence depending on the candidate’s location. Travel requirements are limited to training, according to the job description.

Listed locations include:

• Bangalore, Karnataka

• Hyderabad, Telangana

• Pune, Maharashtra

• Mumbai, Maharashtra

• Remote India

How to Apply

Interested candidates can review the complete job description and apply through Fortrea’s official careers portal.

Apply for Site Navigator I at Fortrea

Applicants should highlight relevant clinical research experience, ICH-GCP knowledge, regulatory documentation skills, site start-up experience, and familiarity with clinical trial workflows in their resumes.

Job Summary

Nova IVF Fertility Recruitment 2026: Multiple Job Openings

Nova IVF Fertility is inviting applications for multiple positions at its Hajipur, Bihar centre. The recruitment drive includes opportunities for Staff Nurses, Pharmacists, Customer Care Executives, Andro Technicians and NFC Executives.
Candidates with qualifications such as GNM, B.Sc Nursing, D.Pharm, B.Pharm, Diploma, B.Sc, M.Sc in Microbiology, M.Sc Life Sciences and other graduate qualifications can apply for suitable roles.
Applicants should have 1–5 years of experience, depending on the position, and nursing or pharmacy candidates must hold the required State Nursing Council or Pharmacy Council registration.
Interested candidates can send their updated CVs to the recruitment email address provided below.

H2: Nova IVF Fertility Recruitment 2026

Nova IVF Fertility has announced openings across clinical support, pharmacy, customer care and laboratory-related functions at its Hajipur centre. Candidates with the required educational qualifications and relevant work experience can apply for the positions listed in the recruitment notice.

H2: Nova IVF Fertility Vacancy Details

Position	Qualification	Experience
Staff Nurse	GNM / B.Sc Nursing	1–3 years
Pharmacist	D.Pharma / B.Pharma	1–5 years
Executive – Customer Care	Diploma / Any Graduate	1–3 years
Andro Technician	B.Sc / M.Sc in Microbiology / M.Sc Life Sciences	2–4 years
Executive – NFC	Any Graduate	1–3 years

H2: Job Role and Responsibilities

H3: Staff Nurse

The Staff Nurse position is suitable for candidates with a GNM or B.Sc Nursing qualification and 1–3 years of experience. Applicants must have the required nursing council registration.

H3: Pharmacist

Candidates with a Diploma in Pharmacy or Bachelor of Pharmacy and 1–5 years of experience can apply for the Pharmacist position. State Pharmacy Council registration is mandatory.

H3: Executive – Customer Care

Candidates with a diploma or any graduate qualification and 1–3 years of experience are eligible to apply for the Customer Care Executive position.

H3: Andro Technician

The Andro Technician role is open to candidates with a B.Sc or M.Sc in Microbiology or an M.Sc in Life Sciences. Applicants should have 2–4 years of relevant experience.

H3: Executive – NFC

Candidates with any graduate qualification and 1–3 years of experience can apply for the NFC Executive position.

H2: Eligibility and Qualifications

Applicants should meet the educational and experience requirements specified for their preferred role.

Eligible qualifications include:

• GNM
• B.Sc Nursing
• D.Pharm
• B.Pharm
• Diploma
• Any Graduate
• B.Sc in Microbiology
• M.Sc in Microbiology
• M.Sc Life Sciences

Important requirement: State Nursing Council registration is mandatory for nursing candidates, and State Pharmacy Council registration is mandatory for pharmacy candidates.

H2: Location and Experience

Job Location: Nova IVF Fertility Centre, Hajipur, Bihar.

Experience requirements vary according to the position:

• Staff Nurse: 1–3 years
• Pharmacist: 1–5 years
• Executive – Customer Care: 1–3 years
• Andro Technician: 2–4 years
• Executive – NFC: 1–3 years

H2: How to Apply

Interested and eligible candidates should follow these steps:

1. Prepare an updated CV with accurate educational qualifications and work experience.
2. Mention the position you are applying for in your email.
3. Send your CV to ipsa.mohanty@novaivffertility.com.
4. For further information, visit the official website: www.novaivffertility.com.

Candidates applying for Staff Nurse and Pharmacist positions should ensure that they meet the applicable registration requirements.

H2: Frequently Asked Questions

H3: 1. Which positions are available at Nova IVF Fertility?

The advertised openings include Staff Nurse, Pharmacist, Executive – Customer Care, Andro Technician and Executive – NFC.

H3: 2. Can freshers apply for these positions?

The advertisement specifies experience requirements ranging from 1–5 years, depending on the position. Freshers are not explicitly listed as eligible.

H3: 3. What qualifications are required for the Pharmacist position?

Candidates need a D.Pharm or B.Pharm qualification and 1–5 years of experience. State Pharmacy Council registration is mandatory.

H3: 4. What is the qualification for the Andro Technician role?

Candidates need a B.Sc or M.Sc in Microbiology or an M.Sc in Life Sciences, along with 2–4 years of experience.

H3: 5. How can candidates apply?

Candidates can email their updated CV to ipsa.mohanty@novaivffertility.com.

H3: 6. Where is the recruitment location?

The openings are for the Nova IVF Fertility centre in Hajipur, Bihar.

H2: Nova IVF Fertility Recruitment Summary

Category	Details
Company	Nova IVF Fertility
Vacancies	Staff Nurse, Pharmacist, Executive – Customer Care, Andro Technician, Executive – NFC
Required Education	GNM, B.Sc Nursing, D.Pharm, B.Pharm, Diploma, Any Graduate, B.Sc / M.Sc Microbiology, M.Sc Life Sciences
Experience	1–5 years, depending on the position

Felix Generics Pvt. Ltd. is conducting a walk-in interview in Ahmedabad for multiple pharmaceutical manufacturing and quality positions at its Pithampur plant.
The recruitment drive includes openings in Injectable Production, Quality Control, Quality Assurance, Technology Transfer, Validation, and OSD Production.
Candidates with ITI, Diploma, D.Pharm, B.Pharm, M.Pharm, M.Sc. Microbiology, M.Sc. Biotechnology, or M.Sc. Chemistry qualifications can apply for relevant positions.
The walk-in interview is scheduled for 25 October 2026 at Pride Plaza Hotel, Judges Bungalow Road, S.G. Road, Bodakdev, Ahmedabad, Gujarat.

Felix Generics Recruitment: Department-Wise Vacancies

Felix Generics Pvt. Ltd. is inviting applications from experienced pharmaceutical professionals for manufacturing, quality, validation, and technology transfer roles. The recruitment covers injectable and oral solid dosage (OSD) operations, with positions ranging from Technician and Officer to Assistant Manager and Deputy Manager.

Walk-In Interview Details

• Company: Felix Generics Pvt. Ltd.
• Recruitment Type: Walk-In Interview
• Interview Date: 25 October 2026, Sunday
• Interview Time: 9:30 AM to 3:30 PM
• Interview Location: Pride Plaza Hotel, Judges Bungalow Road, S.G. Road, Bodakdev, Ahmedabad, Gujarat 380054
• Plant Location: Pithampur
• Contact Numbers: 9109968673, 9109912946, 9109996408
• Resume Email: jobs@felixvet.com

1. Injectable Production Department

Available Positions

• Technician
• Senior Officer
• Executive

Eligibility & Qualifications

• ITI
• Diploma
• B.Pharm
• M.Pharm

Experience: 2–6 years for Technician, 4–5 years for Senior Officer, and 5–8 years for Executive.

Key Responsibilities

Technician

• Handle aseptic filling and filtration operations.
• Operate vial washing and autoclave equipment.
• Work in microsphere manufacturing and controlled areas.

Senior Officer

• Manage packing and labelling areas.
• Perform visual inspection activities.

Executive

• Handle aseptic area operations, including filling, filtration, and capping.

2. Quality Control Microbiology Department (Injectable)

Available Positions

Officer / Senior Executive

Eligibility & Qualifications

• M.Sc. Microbiology
• M.Sc. Biotechnology

Experience: 2–7 years

Key Responsibilities

• Perform microbiological testing, including sterility, BET, MLT, and GPT.
• Conduct method validations.
• Maintain QMS documentation and compliance.
• Support audit readiness, data integrity, and GMP-regulated laboratory operations.

3. Quality Control Department (Injectable)

Available Positions

Officer to Executive

Eligibility & Qualifications

• M.Sc. Chemistry
• M.Pharm
• B.Pharm

Experience: 2–8 years

Key Responsibilities

• Handle and calibrate analytical instruments such as HPLC, GC, FTIR, UV, auto-titrators, and KF equipment.
• Perform analysis of raw materials, water, finished products, and stability samples.

4. Quality Assurance Department (Injectable)

Available Positions

Officer to Senior Executive

Eligibility & Qualifications

• M.Pharm
• B.Pharm

Experience: 2–8 years

Key Responsibilities

• Perform IPQA activities, including line clearance, sampling, and in-process checks.
• Handle AQL and media fills.
• Support aseptic supervision and batch record review.
• Conduct audit trail reviews and batch release activities.
• Manage document collection, issuance, retrieval, and archiving.
• Prepare and review SOPs.

Candidates should have a strong understanding of good manufacturing practices.

5. Technology Transfer Department (OSD)

Available Positions

Assistant Manager / Deputy Manager

Eligibility & Qualifications

• M.Pharm
• B.Pharm

Experience: 10–14 years

Key Responsibilities

• Support technology transfer and process optimization.
• Perform validation activities.
• Apply knowledge of cGMP and regulatory guidelines.
• Prepare, review, and approve GMP documents, including SOPs, BMR/BPR, protocols, and reports.
• Handle change controls, risk assessments, QRM, deviations, and investigations.

6. Validation Department (OSD)

Available Positions

Officer to Deputy Manager

Eligibility & Qualifications

• M.Pharm
• B.Pharm

Experience: 4–15 years

Key Responsibilities

• Handle greenfield project activities.
• Support equipment qualification and computer system validation.
• Work on HVAC and water system qualification.
• Support compressed air and nitrogen system qualification.
• Handle temperature mapping.

7. Quality Control Department (OSD)

Available Positions

Officer to Senior Executive

Eligibility & Qualifications

• M.Sc.
• M.Pharm
• B.Pharm

Experience: 4–7 years

Key Responsibilities

• Perform routine and non-routine quality control testing of raw materials, in-process samples, and finished products.
• Use analytical instruments and techniques, including HPLC, GC, UV, KF, potentiometers, IR, dissolution, and Malvern Mastersizer.
• Ensure compliance with SOPs, GLP, and regulatory standards.
• Perform method validation, verification, and transfer activities according to ICH guidelines.
• Prepare and review analytical method validation, verification, and transfer protocols.

8. Production Department (OSD)

Available Positions

• Executive (Granulation / Compression / Packing)
• Officer (Granulation / Compression / Coating / Liquid & Paste Manufacturing / Packing)
• Technician (Granulation / Compression / Coating / Liquid & Paste Manufacturing / Liquid Filling / Bottle Primary Packing)

Eligibility & Qualifications

• M.Pharm
• B.Pharm
• D.Pharm
• Diploma
• ITI

Experience Requirements

• Executive: 4–7 years
• Officer: 2–4 years
• Technician: 2–6 years

Key Responsibilities

Executive and Officer Roles

• Work in pharmaceutical OSD manufacturing operations.
• Support granulation, compression, coating, and packing activities.
• Follow manufacturing procedures and documentation requirements.

Technician Role

• Operate granulation equipment independently.
• Perform spraying and roll compaction activities.
• Handle liquid and paste manufacturing equipment.
• Work in primary bottle packing, liquid filling, and related operations.
• Follow machine operation, cleaning, changeover, and alarm-handling procedures.

Candidates should have exposure to an USFDA-approved or EUGMP-approved company. Experience with material handling, electronic batch records, SAP, machine alarms, QMS, deviations, change control, SOPs, daily reports, and manpower handling is relevant to the listed roles.

Eligibility & Qualifications: Quick Overview

Department	Qualifications	Experience
Injectable Production	ITI, Diploma, B.Pharm, M.Pharm	2–8 years, depending on position
QC Microbiology (Injectable)	M.Sc. Microbiology, M.Sc. Biotechnology	2–7 years
QC (Injectable)	M.Sc. Chemistry, M.Pharm, B.Pharm	2–8 years
QA (Injectable)	M.Pharm, B.Pharm	2–8 years
Technology Transfer (OSD)	M.Pharm, B.Pharm	10–14 years
Validation (OSD)	M.Pharm, B.Pharm	4–15 years
QC (OSD)	M.Sc., M.Pharm, B.Pharm	4–7 years
Production (OSD)	M.Pharm, B.Pharm, D.Pharm, Diploma, ITI	2–7 years, depending on position

How to Apply

Interested candidates can attend the walk-in interview at the venue mentioned below. Candidates who cannot attend can send their resumes to the recruitment email address provided in the advertisement.

Walk-In Interview Address

Pride Plaza Hotel
Judges Bungalow Road, S.G. Road, Bodakdev, Ahmedabad, Gujarat 380054.

Date: 25 October 2026
Time: 9:30 AM to 3:30 PM

Application by Email

Send your updated resume to jobs@felixvet.com.

Documents to Carry

• Updated resume
• Educational certificates
• Relevant experience documents
• Government-issued identity proof
• Supporting documents for relevant technical skills and training

Additional Requirements

• Candidates should have experience in an USFDA-approved company.
• Good communication skills are required.
• Candidates who cannot attend the interview may email their resumes to the recruitment address.
• Confirm the exact designation and department requirements before attending.

Frequently Asked Questions

1. Which company is conducting the walk-in interview?

Felix Generics Pvt. Ltd. is conducting the recruitment drive for its Pithampur plant.

2. When is the walk-in interview scheduled?

The interview is scheduled for 25 October 2026, from 9:30 AM to 3:30 PM.

3. Where will the interview take place?

The venue is Pride Plaza Hotel, Judges Bungalow Road, S.G. Road, Bodakdev, Ahmedabad, Gujarat 380054.

4. Which qualifications are accepted?

The advertisement lists ITI, Diploma, D.Pharm, B.Pharm, M.Pharm, M.Sc. Microbiology, M.Sc. Biotechnology, and M.Sc. Chemistry for relevant roles.

5. What is the experience requirement?

The listed experience requirements range from 2 to 15 years, depending on the department and designation.

6. How can candidates apply if they cannot attend?

Candidates who cannot attend the walk-in interview can send their resumes to jobs@felixvet.com.

Job Summary

Category	Details
Company	Felix Generics Pvt. Ltd.
Vacancies	Technician, Officer, Senior Officer, Executive, Assistant Manager, Deputy Manager, Senior Executive
Required Education	ITI, Diploma, D.Pharm, B.Pharm, M.Pharm, M.Sc. Microbiology, M.Sc. Biotechnology, M.Sc. Chemistry
Experience	2–15 years, depending on the role

Torrent Pharmaceuticals Walk-In Interview for Production, Quality Control and Quality Assurance Jobs

Torrent Pharmaceuticals is inviting applications for multiple pharmaceutical manufacturing and quality-related positions at its Baddi, Himachal Pradesh, and Indrad, Gujarat, facilities.
The recruitment drive includes openings in Quality Control, Microbiology, Quality Assurance, Production, Engineering, and Supply Chain Management.
Candidates with B.Sc, M.Sc, B.Pharm, M.Pharm, B.E., and relevant ITI qualifications can apply for suitable positions based on their experience.
The walk-in interview is scheduled for 25 October 2026 at Torrent Pharmaceuticals Limited, Baddi, Himachal Pradesh, from 9:00 AM to 2:00 PM.

Torrent Pharmaceuticals Recruitment: Department-Wise Vacancies

Torrent Pharmaceuticals is hiring candidates for pharmaceutical manufacturing, laboratory testing, quality assurance, engineering, and production planning activities. The advertised openings cover both experienced professionals and eligible trainees.

1. Torrent Pharmaceuticals Baddi Recruitment

Position: Executive / Technical Assistant

Department: Quality Control

Qualification: B.Sc / M.Sc / B.Pharm

Experience: 2–7 years

Key Responsibilities and Required Skills

• Analysis of finished products, stability samples, and raw materials.
• Knowledge of analytical method validation, verification, and method transfer.
• Familiarity with HPLC, GC, UV spectroscopy, and other analytical instruments.
• Understanding of laboratory practices, documentation, and regulatory requirements.
• Knowledge of data integrity and troubleshooting.

How to Apply

Candidates who cannot attend the walk-in interview may send their resumes to:

Email: recruitmentbaddi@torrentpharma.com

2. Torrent Pharmaceuticals Panoli Recruitment

Job Location: Panoli, Ankleshwar, Gujarat

Quality Control (Formulation)

Designation: Officer / Executive

Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm

Experience: 1–7 years

Job Description: Experience in HPLC, GC, GLP, and analytical method validation.

Quality Control – Microbiology

Designation: Officer / Executive

Qualification: B.Sc / M.Sc (Microbiology)

Experience: 2–6 years

Job Description: Experience in microbiological method validation and media preparation.

Quality Assurance (OSD)

Designation: Officer / Executive

Qualification: B.Pharm / M.Pharm / M.Sc

Experience: 1–5 years

Job Description: Experience in IPQA and OSD documentation.

Quality Assurance (Liquid)

Designation: Officer / Executive

Qualification: B.Pharm / M.Pharm / M.Sc

Experience: 1–5 years

Job Description: Experience in IPQA and liquid manufacturing documentation.

Quality Assurance (Injectable)

Designation: Officer / Executive

Qualification: B.Pharm / M.Pharm / M.Sc

Experience: 1–5 years

Job Description: Experience in IPQA documentation for injectable manufacturing.

Production – OSD Formulation

Designation: Officer / Executive

Qualification: B.Pharm / M.Pharm

Experience: 2–6 years

Job Description: Experience in pharmaceutical manufacturing and packing documentation.

Liquid (Oral) Manufacturing

Designation: Officer / Executive

Qualification: B.Pharm / M.Pharm

Experience: 1–6 years

Job Description: Experience in oral liquid manufacturing, packaging, and documentation.

Production (Injectable)

Designation: Officer / Executive

Qualification: B.Pharm / M.Pharm

Experience: 2–6 years

Job Description: Experience in LVP, SVP manufacturing, and aseptic packaging operations.

Supply Chain Management – Production Planning

Designation: Officer / Executive

Qualification: B.Pharm / M.Pharm / MBA

Experience: 2–6 years

Job Description: Material planning, inventory monitoring, and production planning activities.

Production (ITI)

Designation: Trainee Junior Officer

Qualification: ITI (2 years completed in any trade)

Experience: 0–5 years

Job Description: Work in OSD and injectable plants as an Operator or Technician.

Engineering – Formulation Instrumentation

Designation: Officer / Executive

Qualification: B.E. (Instrumentation)

Experience: 3–7 years

Job Description: Maintenance of plant machinery, calibration, and instrumentation for OSD and injectable plants.

Engineering – Formulation Mechanical

Designation: Officer / Executive

Qualification: B.E. (Mechanical)

Experience: 3–7 years

Job Description: Knowledge of OSD and injectable plant maintenance.

Engineering – Formulation Electrical

Designation: Officer / Executive

Qualification: B.E. (Electrical)

Experience: 3–7 years

Job Description: Electrical maintenance of formulation and injectable plants.

Eligibility & Qualifications

Candidates should possess the educational qualifications and relevant experience specified for their preferred department.

Qualifications mentioned in the recruitment advertisement:

B.Sc | M.Sc | B.Pharm | M.Pharm | MBA | B.E. (Instrumentation) | B.E. (Mechanical) | B.E. (Electrical) | ITI

Experience requirements vary by position, ranging from fresher-level eligibility for the Production (ITI) trainee role to 7 years for certain laboratory and engineering positions.

How to Apply

Interested candidates should attend the walk-in interview on 25 October 2026, Sunday, from 9:00 AM to 2:00 PM.

Walk-In Interview Venue

Torrent Pharmaceuticals Limited
Near Baddi University, Village – Bhud, Makhnu Majra, Tehsil – Baddi, District – Solan, Himachal Pradesh 173205.

Candidates unable to attend the Panoli recruitment drive may send their resumes to:

Email: NavneetKaur@torrentpharma.com

Documents to Carry

• Updated resume
• Educational certificates
• Relevant experience documents
• Government-issued identity proof

Candidates should confirm the applicable location and role requirements before attending.

Frequently Asked Questions

1. Which company is conducting the walk-in interview?

Torrent Pharmaceuticals is conducting recruitment for Quality Control, Quality Assurance, Production, Microbiology, Engineering, and Supply Chain Management positions.

2. What is the walk-in interview date?

The interview is scheduled for 25 October 2026, Sunday.

3. Which qualifications are accepted?

The listed qualifications include B.Sc, M.Sc, B.Pharm, M.Pharm, MBA, B.E. in relevant engineering disciplines, and ITI.

4. Can freshers apply?

The Production (ITI) Trainee Junior Officer position lists an experience range of 0–5 years. Candidates should confirm the specific eligibility criteria before applying.

5. What is the experience requirement?

Experience requirements vary by position, ranging from 0–5 years for the Production (ITI) trainee role to 1–7 years for several technical positions.

6. Where is the Baddi interview venue?

The venue is Torrent Pharmaceuticals Limited, near Baddi University, Village Bhud, Makhnu Majra, Tehsil Baddi, District Solan, Himachal Pradesh 173205.

Job Summary

Category	Details
Company	Torrent Pharmaceuticals
Vacancies	Executive, Technical Assistant, Officer, Trainee Junior Officer
Required Education	B.Sc, M.Sc, B.Pharm, M.Pharm, MBA, B.E. (Instrumentation / Mechanical / Electrical), ITI
Experience	0–7 years, depending on the position

Syneos Health Recruitment – Drug Safety Specialist I / II

Syneos Health is hiring Drug Safety Specialist I / II professionals for its pharmacovigilance operations in Hyderabad and Gurugram, India. This full-time, permanent opportunity is suitable for candidates with 1–6 years of experience in drug safety, individual case safety report (ICSR) processing, and pharmacovigilance activities. The role involves processing spontaneous, clinical trial, and literature cases, performing medical coding and narrative writing, and ensuring compliance with global pharmacovigilance guidelines. Candidates with relevant Pharmacy, Medical, Dental, or Homeopathic qualifications can review the job requirements and apply.

Company Overview

Syneos Health is a contract research and healthcare services company operating in the clinical research and life sciences industry. The company supports clinical development and related healthcare activities, including drug safety and pharmacovigilance operations.

Job Details

Job Role & Responsibilities

The Drug Safety Specialist I / II will support end-to-end individual case safety report processing and pharmacovigilance activities.

Key responsibilities include:

• Perform end-to-end ICSR case processing for spontaneous, clinical trial, and literature cases.

• Execute accurate data entry activities, particularly during the initial phase of the role.

• Manage case workflows, including triage, data entry, coding, narrative writing, and submission readiness.

• Ensure compliance with global pharmacovigilance guidelines, standard operating procedures (SOPs), and applicable regulatory requirements.

• Perform quality checks on processed safety cases based on experience and performance.

Eligibility & Qualifications

Candidates with the following educational qualifications are listed in the job advertisement.

Undergraduate qualifications:

• BHMS – Bachelor of Homeopathic Medicine and Surgery.

• BDS – Bachelor of Dental Surgery.

• B.Pharm – Bachelor of Pharmacy, including Pharmaceutical Analysis and Quality Assurance specializations.

Postgraduate qualifications:

• M.Pharm – Master of Pharmacy.

• MDS – Master of Dental Surgery.

Candidates should verify the accepted qualification and specialization requirements in the original listing before applying.

Experience Requirements

• Experience range: 1–6 years.

• Relevant experience in drug safety, pharmacovigilance, or ICSR case processing is applicable to the role.

• Candidates should be familiar with safety case workflows and regulatory documentation.

Required Skills

The job advertisement highlights the following skills:

• Drug Safety

• Pharmacovigilance

• ICSR case processing

• Clinical trial case processing

• Literature case processing

• Narrative writing

• Case data entry and coding

• Case triage and submission readiness

• Quality checks and regulatory compliance

Job Locations

The position is listed for the following locations:

• Hyderabad, Telangana

• Gurugram, Haryana

The advertisement lists the role as full-time and permanent.

How to Apply

Interested candidates can review the complete job description and submit their application through Naukri.

Apply for Drug Safety Specialist I / II at Syneos Health

Applicants should highlight their pharmacovigilance experience, ICSR case processing skills, medical coding knowledge, and narrative writing experience in their resumes.

Job Summary